To Characterize the Safety and Tolerability of Eculizumab in Two Japanese aHUS Patients

NCT01755429 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2

Last updated 2012-12-24

No results posted yet for this study

Summary

This protocol is intended to formally collect data on the treatment of aHUS with eculizumab in Japanese patients.

Conditions

  • ATYPICAL HEMOLYTIC UREMIC SYNDROME (AHUS)

Sponsors & Collaborators

  • Alexion Pharmaceuticals, Inc.

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-05-31
Primary Completion
2012-05-31
Completion
2012-07-31

Countries

  • Japan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01755429 on ClinicalTrials.gov